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PUBMED FOR HANDHELDS

Journal Abstract Search


126 related items for PubMed ID: 6814490

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  • 22. Alpha-thalassemia and the production of different alpha chain variants in heterozygotes.
    Felice AE, Webber BB, Huisman TH.
    Biochem Genet; 1981 Jun; 19(5-6):487-98. PubMed ID: 7295286
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  • 23. A heterozygote for Hb S beta, Hb C beta and Hb G Philadelphia beta in a family presenting evidence for heterogeneity of hemoglobin alpha chain loci.
    Rucknagel DL, Rising JA.
    Am J Med; 1975 Jul; 59(1):53-60. PubMed ID: 1138551
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  • 24. Hb A2-Canada or alpha 2 delta 2 99(G1) Asp replaced by Asn, a newly discovered delta chain variant with increased oxygen affinity occurring in cis to beta-thalassemia.
    Salkie ML, Gordon PA, Rigal WM, Lam H, Wilson JB, Headlee ME, Huisman TH.
    Hemoglobin; 1982 Jul; 6(3):223-31. PubMed ID: 7129931
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  • 25. Hb Tak confirmed by DNA analysis: not expressed as thalassemia in a Hb Tak/Hb E compound heterozygote.
    Hoyer JD, Wick MJ, Thibodeau SN, Viker KA, Conner R, Fairbanks VF.
    Hemoglobin; 1998 Jan; 22(1):45-52. PubMed ID: 9494047
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  • 29. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
    Harteveld CL, Versteegh FG, Kok PJ, van Rooijen-Nijdam IH, van Delft P, Giordano PC.
    Hemoglobin; 2006 Jan; 30(3):349-54. PubMed ID: 16840225
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  • 34. Hemoglobin Evanston: alpha 14(A12) Trp leads to Arg. A variant hemoglobin associated with alpha-thalassemia-2.
    Moo-Penn WF, Baine RM, Jue DL, Johnson MH, McGuffey JE, Benson JM.
    Biochim Biophys Acta; 1983 Sep 14; 747(1-2):65-70. PubMed ID: 6882779
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